A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids

A randomization-based causal inference framework for uncovering environmental exposure effects on human gut microbiota

Alcohol consumption is associated with widespread changes in blood DNA methylation: analysis of cross-sectional and longitudinal data

An integrative analysis of clinical and epigenetic biomarkers of mortality

Association analysis between an epigenetic alcohol risk score and blood pressure

Better ageing with personalized lifestyle support from a health coach using a digital app – a population-based intervention study in Germany

Breaking the Norm: Population-Scale Normative Modeling of Brain Structure in Depression and Anxiety

CODI: Enhancing machine learning-based molecular profiling through contextual out-of-distribution integration

Circulating interleukin-6 levels and incident ischemic stroke: a systematic review and meta-analysis of population-based cohort studies

Circulating metabolites modulated by diet are causally associated with depression

DNA methylation signature of chronic low-grade inflammation and its role in cardio-respiratory diseases

Determinants of ascending aortic morphology: Cross-sectional deep learning-based analysis on 25,073 non-contrast-enhanced MRI of NAKO

Development and validation of DNA Methylation scores in two European cohorts augment 10-year risk prediction of type 2 diabetes

Distribution and associated factors of hepatic iron – a population-based imaging study

Epigenetic scores for the circulating proteome as tools for disease prediction

Genetic Contributions to Early and Late Onset Ischemic Stroke

Genome-wide analysis in over 1 million individuals reveals over 2,000 independent genetic signals for blood pressure

Implicating genes, pleiotropy and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis

Individual bioenergetic capacity as a potential source of resilience to Alzheimer’s disease

Mendelian Randomization evaluation of causal effects of fibrinogen on incident coronary heart disease

Methylation status of VTRNA2-1/nc886 is stable across human populations, monozygotic twin pairs and in majority of somatic tissues

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 210 loci underlying cardiac conduction

Proteogenomic integration reveals CXCL10 as a potentially downstream causal mediator for IL-6 signaling on atherosclerosis

Proteomic Signatures as Biomarkers of Atherosclerosis Burden

Stroke genetics informs drug discovery and risk prediction across ancestries

The mediating role of epigenetic clocks underlying educational inequalities in mortality: a multi-cohort study